Theme Cancer, Karolinska University Hospital, Stockholm, Sweden.
Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Oncoimmunology. 2024 Jul 3;13(1):2372875. doi: 10.1080/2162402X.2024.2372875. eCollection 2024.
Immune checkpoint inhibitors (ICIs) are linked to diverse immune-related adverse events (irAEs). Rare irAEs surface first in clinical practice. Here, we systematically studied the rare irAE, cytokine-release syndrome (CRS), in a cohort of 2672 patients treated with ICIs at Karolinska University Hospital in Stockholm, Sweden. We find that the risk of ICI-induced CRS - defined as fever, negative microbiological findings and absence of other probable causes within 30 days after ICI treatment - is approximately 1%, higher than previously reported. ICI-induced CRS was often mild and rechallenge with ICIs after mild CRS was generally safe. However, two out of 28 patients experienced high-grade CRS, and one was fatal. While C-reactive protein (CRP) and procalcitonin were not discriminative of fatal CRS, our data suggest that the quick Sequential Organ Failure Assessment (qSOFA) score might identify high-risk patients. These data provide a framework for CRS risk assessment and motivate multicenter studies to improve early CRS diagnosis.
免疫检查点抑制剂(ICIs)与多种免疫相关不良事件(irAEs)有关。罕见的 irAEs 首先在临床实践中出现。在这里,我们在斯德哥尔摩卡罗林斯卡大学医院的 2672 名接受 ICI 治疗的患者队列中系统地研究了罕见的 irAE,细胞因子释放综合征(CRS)。我们发现,ICI 诱导的 CRS 的风险 - 定义为在 ICI 治疗后 30 天内发热、微生物学检查结果阴性且无其他可能原因 - 约为 1%,高于先前报道。ICI 诱导的 CRS 通常较轻,轻度 CRS 后再次使用 ICI 通常是安全的。然而,28 名患者中有 2 名出现了重度 CRS,其中 1 名死亡。虽然 C 反应蛋白(CRP)和降钙素原不能区分致命性 CRS,但我们的数据表明,快速序贯器官衰竭评估(qSOFA)评分可能可以识别高危患者。这些数据为 CRS 风险评估提供了框架,并促使多中心研究以改善早期 CRS 的诊断。